Adult-onset of Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) Syndrome Presenting as Acute Meningoencephalitis: A Case Report-Reference-Cited by-同舟云学术

Adult-onset of Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) Syndrome Presenting as Acute Meningoencephalitis: A Case Report

Published:2012-09 Issue:3 Volume:43 Page:e163-e166
ISSN:0736-4679
Container-title:The Journal of Emergency Medicine
language:en
Short-container-title:The Journal of Emergency Medicine

Author:

Hsu Yu-Chuan,Yang Fu-Chi,Perng Cherng-Lih,Tso An-Chen,Wong Lee-Jun C.,Hsu Chang-Hung

Publisher

Elsevier BV

Subject

Emergency Medicine

Reference25 articles.

1. Mitochondrial myopathy, encephalopathy, lactic acidosis and strokelike episodes: a distinctive clinical syndrome;Pavlakis;Ann Neurol,1984

2. Molecular pathology of MELAS and MERRF;Chinnery;Brain,1997

3. Mitochondrial DNA and disease;Dimauro;Ann Med,2005

4. Valproate as a cause of hyperammonemia in heterozygotes with ornithine-transcarbamylase deficiency;Leão;Neurology,1995

5. Valproic acid aggravates epilepsy due to MELAS in a patient with an A3243G mutation of mitochondrial DNA;Lin;Metab Brain Dis,2007

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